%D9%84%D9%88%D8%AA%D8%A6%D9%88%D9%84%DB%8C%D9%86LuteolinaCategory:LuteolinLuteolin%CE%9B%CE%BF%CF%85%CF%84%CE%B5%CE%BF%CE%BB%CE%AF%CE%BD%CE%B7LuteolinLuteolinoLuteolina%D9%84%D9%88%D8%AA%D8%A6%D9%88%D9%84%DB%8C%D9%86LuteoliiniLut%C3%A9olineLuteolina%E3%83%AB%E3%83%86%E3%82%AA%E3%83%AA%E3%83%B3LuteolinasLuteolineLuteolinaLuteolinLuteolinLuteolinLuteolinQ415011%E6%9C%A8%E7%8A%80%E8%8D%89%E7%B4%A0
about
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Luteolin, a flavonoid with potential for cancer prevention and therapyModulatory effect of luteolin on redox homeostasis and inflammatory cytokines in a mouse model of liver cancerLuteolin Attenuates Airway Mucus Overproduction via Inhibition of the GABAergic SystemAnti-carcinogenic effects of the flavonoid luteolin.Regulation of Sirt1/Nrf2/TNF-α signaling pathway by luteolin is critical to attenuate acute mercuric chloride exposure induced hepatotoxicity.Effects of Luteolin and Quercetin in Combination with Some Conventional Antibiotics against Methicillin-Resistant Staphylococcus aureus.Luteolin protects mice from severe acute pancreatitis by exerting HO-1-mediated anti-inflammatory and antioxidant effectsLuteolin inhibits lung metastasis, cell migration, and viability of triple-negative breast cancer cells.At the crossroads from bench to bedside: luteolin is a promising pharmacological agent against myocardial ischemia reperfusion injury.Anti-inflammatory effects of luteolin on experimental autoimmune thyroiditis in mice.Luteolin improves cardiac dysfunction in heart failure rats by regulating sarcoplasmic reticulum Ca2+-ATPase 2a.Drugs and drug-like molecules can modulate the function of mucosal-associated invariant T cells.Anticancer activity of baicalein and luteolin studied in colorectal adenocarcinoma LoVo cells and in drug-resistant LoVo/Dx cells.Effects of Catechol O-Methyl Transferase Inhibition on Anti-Inflammatory Activity of Luteolin Metabolites.Anticancer effect of luteolin is mediated by downregulation of TAM receptor tyrosine kinases, but not interleukin-8, in non-small cell lung cancer cells.Dietary Flavonoids Luteolin and Quercetin Suppressed Cancer Stem Cell Properties and Metastatic Potential of Isolated Prostate Cancer Cells.Luteolin suppresses the JAK/STAT pathway in a cellular model of intestinal inflammation.Preparation and Characterization of Copolymer Micelles for the Solubilization and In Vitro Release of Luteolin and Luteoloside.Neuroprotective effects of luteolin against apoptosis induced by 6-hydroxydopamine on rat pheochromocytoma PC12 cells.The flavonoids diosmetin and luteolin exert synergistic cytostatic effects in human hepatoma HepG2 cells via CYP1A-catalyzed metabolism, activation of JNK and ERK and P53/P21 up-regulation.Luteolin, a food-derived flavonoid, suppresses adipocyte-dependent activation of macrophages by inhibiting JNK activation.Luteolin inhibits invasion of prostate cancer PC3 cells through E-cadherin.Protective Effects of Luteolin on Lipopolysaccharide-Induced Acute Renal Injury in Mice.Luteolin ameliorates colistin-induced nephrotoxicity in the rat models.Investigation of the anxiolytic effects of luteolin, a lemon balm flavonoid in the male Sprague-Dawley rat.Study of antioxidant effect of apigenin, luteolin and quercetin by DNA protective method.Luteolin reduces lipopolysaccharide-induced lethal toxicity and expression of proinflammatory molecules in mice.Solubility enhancement of a hydrophobic flavonoid, luteolin by the complexation with cyclosophoraoses isolated from Rhizobium meliloti.Simultaneous Ultra Performance Liquid Chromatography Determination and Antioxidant Activity of Linarin, Luteolin, Chlorogenic Acid and Apigenin in Different Parts of Compositae Species.In Vivo Selective Capture and Rapid Identification of Luteolin and Its Metabolites in Rat Livers by Molecularly Imprinted Solid-Phase Microextraction.Investigating the inhibitory activity and mechanism differences between norartocarpetin and luteolin for tyrosinase: A combinatory kinetic study and computational simulation analysis.Assessment of luteolin isolated from Eclipta alba leaves in animal models of epilepsy.Luteolin suppresses the metastasis of triple-negative breast cancer by reversing epithelial-to-mesenchymal transition via downregulation of β-catenin expression.Two dietary polyphenols, fisetin and luteolin, reduce inflammation but augment DNA damage-induced toxicity in human RPE cells.Metabolic Disposition of Luteolin Is Mediated by the Interplay of UDP-Glucuronosyltransferases and Catechol-O-Methyltransferases in Rats.Active Compounds Derived from Fuzheng Huayu Formula Protect Hepatic Parenchymal Cells from Apoptosis Based on Network Pharmacology and Transcriptomic AnalysisSerum Concentration of Genistein, Luteolin and Colorectal Cancer PrognosisThe Flavone Luteolin, an Endocrine Disruptor, Relaxed Male Guinea Pig Gallbladder StripsLuteolin induces hippocampal neurogenesis in the Ts65Dn mouse model of Down syndromeLuteolin suppresses tumor proliferation through inducing apoptosis and autophagy via MAPK activation in glioma
P921
Q24652632-ADB976B6-4146-4F03-8EFD-052919FB956BQ28468620-D068EEC4-2212-44C9-8045-C68E6CA297DDQ37232960-9836C0AD-9EE2-4EC1-8458-43E847A490B3Q37306454-BB5C08DD-A1C4-4FC3-8775-E0A91992E1B4Q37419174-61324424-CFCA-4348-8A7A-6743C203837FQ37465764-101F5014-9392-4E09-8CFA-501E733D7C07Q37527788-993F05A4-D81B-4977-BE4C-C0D3ECFB9868Q37551677-A77ECA10-FFA7-4FD4-8FA2-543AE7577837Q37570347-979CABE8-3C7D-45B8-91E7-11A6FE6DE866Q37582009-CB451EEE-2F95-4E0B-A505-BB8A0BE3D76FQ37598388-FCB140EF-BE54-49EE-8050-F81EE7A2C3CAQ38717713-7380DAC4-A54E-4F38-877C-455E5DFA6F0EQ38720136-E9667FB9-41A2-4E79-B80D-897A2179E81EQ38722127-A28C719B-AC75-47BB-BE9F-8D41AEDC1BCEQ38723690-E72734ED-BBC6-41BD-B5C9-4AFEF2470E06Q38727521-1CE51B9F-AA11-42CF-9F5C-C64F786A5DD8Q38773024-E95E89B3-E53C-4AEF-B2CD-E89B789C4765Q39076060-AC35D218-8C56-4D47-8C0C-F7BC2F09891CQ39266111-EE296327-3755-4183-9DD4-D5E86A61D934Q39322406-300A6C24-8674-49EE-AF6D-313173A5C080Q39783870-51C1FA52-B876-4DD1-B3C6-D9C51652F4C1Q39840544-1455C9BE-FFF9-4D51-AF36-ECE4DF81E988Q40393290-040AAAB8-DF89-4564-B90D-59A1C72EF591Q40495606-0F667E45-7AFB-46E1-9302-186C3490B0C3Q42614055-DDCD7AE5-80D6-4333-A859-B02EA2614519Q43691390-8AF07834-0039-44CB-94FD-81EFB2BDB8E1Q43919941-231E2C5A-6F92-4CEE-9212-4F792B55D224Q44628757-BC8DF0E3-A658-4AD3-9C63-3028CCABCC43Q46454795-471EB091-F94A-4E43-BC02-AA3FE3D88EB6Q47339035-2BE8DBEC-9BC0-431A-9213-46C49FD5B556Q47844336-F7C7DA28-578B-44DA-97BB-F99A551713EFQ48403191-877E18E2-1146-493B-8F19-13695145FD1DQ51014562-CD1F5CBB-66F8-4C9D-8114-42558EACA79CQ51173877-CC84F1DA-1048-4A25-A676-6D8BBDB4EEF6Q53605256-E6EFBEA9-909C-4D85-89B5-F33744F15538Q61813625-3D34B792-0F79-4AE5-9F10-4D97CD47E961Q62583148-387C5C98-5702-404B-96B6-895AD9075679Q64068960-F5032C91-A65A-4344-B2D7-3246DA16A393Q64096338-439EA8A5-3E80-4148-84E1-8C10FC5F7A0DQ64108360-1C10512D-9C13-44CA-9FCF-90BF0811C973
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de-ch
chemische verbinding
@nl
component quimic
@oc
name
Luteoliini
@fi
Luteolin
@de
Luteolin
@sh
Luteolin
@sr
Luteolin
@sv
Luteolin
@vi
Luteolina
@ca
Luteolina
@es
Luteolinas
@lt
Luteoline
@nl
type
label
Luteoliini
@fi
Luteolin
@de
Luteolin
@sh
Luteolin
@sr
Luteolin
@sv
Luteolin
@vi
Luteolina
@ca
Luteolina
@es
Luteolinas
@lt
Luteoline
@nl
altLabel
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-benzopyrone
@en
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
@en
C15H10O6
@it
Luteolol
@en
Lutéolol
@fr
Salifazide
@en
digitoflavone
@en
flacitran
@en
毛地黄黄酮
@zh
prefLabel
Luteoliini
@fi
Luteolin
@de
Luteolin
@sh
Luteolin
@sr
Luteolin
@sv
Luteolin
@vi
Luteolina
@ca
Luteolina
@es
Luteolinas
@lt
Luteoline
@nl